4k2y: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
m Protected "4k2y" [edit=sysop:move=sysop]
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''
{{STRUCTURE_4k2y|  PDB=4k2y  |  SCENE=  }}
===Crystal Structure of Human Chymase in Complex with Fragment Inhibitor 6-chloro-1,3-dihydro-2H-indol-2-one===
{{ABSTRACT_PUBMED_23659209}}


The entry 4k2y is ON HOLD
==Function==
[[http://www.uniprot.org/uniprot/CMA1_HUMAN CMA1_HUMAN]] Major secreted protease of mast cells with suspected roles in vasoactive peptide generation, extracellular matrix degradation, and regulation of gland secretion.


Authors: Collins, B.K., Padyana, A.K.
==About this Structure==
[[4k2y]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4K2Y OCA].  


Description: Crystal structure of human chymase with bound inhibitor 6-chloro-1,3-dihydro-indol-2-one
==Reference==
<ref group="xtra">PMID:023659209</ref><references group="xtra"/><references/>
[[Category: Chymase]]
[[Category: Homo sapiens]]
[[Category: Collins, B K.]]
[[Category: Padyana, A K.]]
[[Category: Glycosylated]]
[[Category: Hydrolase-hydrolase inhibitor complex]]
[[Category: Mast cell]]
[[Category: Secreted]]
[[Category: Serine protease]]

Revision as of 15:48, 19 June 2013

Template:STRUCTURE 4k2y

Crystal Structure of Human Chymase in Complex with Fragment Inhibitor 6-chloro-1,3-dihydro-2H-indol-2-one

Template:ABSTRACT PUBMED 23659209

Function

[CMA1_HUMAN] Major secreted protease of mast cells with suspected roles in vasoactive peptide generation, extracellular matrix degradation, and regulation of gland secretion.

About this Structure

4k2y is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Taylor SJ, Padyana AK, Abeywardane A, Liang S, Hao MH, De Lombaert S, Proudfoot JR, Farmer BS, Li X, Collins B, Albaugh DR, Martin L, Hill-Drzewi M, Pullen SS, Takahashi H. Discovery of Potent, Selective Chymase Inhibitors via Fragment Linking Strategies. J Med Chem. 2013 May 9. PMID:23659209 doi:10.1021/jm400138z

Proteopedia Page Contributors and Editors (what is this?)

OCA